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PSA: ½ð±Ò+1, ÐÁ¿à£¬Ð»Ð»£¡ 2014-02-28 10:34:59
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²éѯ½á¹û£º¹²²éµ½598¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . laurotetanine ÏàËÆ¶È:100% Acta Pharmaceutica Sinica 2005 Vol 40 931-934 Alkaloids from the root of Lindera angustifolia ZHAO Qi-zhi; ZHAO Yi-min; WANG Ke-jun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . norglaucine C20H23O4N ÏàËÆ¶È:80% Journal of Natural Products 1979 Vol 42 325-360 porphine Alkaloids. II H¨¦l¨¨ne Guinaudeau, Michel Leboeuf, Andr¨¦ Cav¨¦ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-iodoboldine-HBr.H2O C19H20INO4aHBraH2O ÏàËÆ¶È:68.4% Journal of Natural Products 2000 63 480-484 Halogenated Boldine Derivatives with Enhanced Monoamine Receptor Selectivity Eduardo M. Sobarzo-S¨¢nchez, Jeannette Arbaoui, Philippe Protais, and Bruce K. Cassels Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . (+)-manibacanine ÏàËÆ¶È:68.4% Canadian Journal of Chemistry 1993 71 1128-1135 Nouveaux alcaloïdes isoquinol¨¦iques isol¨¦s d'une Lauraceae bolivienne: Aniba canelilla H.B.K. Jean-Michel Oger, Agn¨¨s Fardeau, Pascal Richomme, H¨¦l¨¨ne Guinaudeau, Alain Fournet Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 1-(4-aminophenyl)-3-(4-(2-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)ethyl)phenyl)urea C26H30N4O3 ÏàËÆ¶È:63.6% Bioorganic & Medicinal Chemistry 2009 17 2524-2535 Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators Werner Klinkhammer, Henrik M¨¹ller, Christoph Globisch, Ilza K. Pajeva, Michael Wiese Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 3-Chloro-4,4',5-trimethoxy-3'-hydroxy-Z-stilbene C17H17ClO4 ÏàËÆ¶È:63.1% Journal of Natural Products 2005 68 1450-1458 Antineoplastic Agents. 509. Synthesis of Fluorcombstatin Phosphate and Related 3-Halostilbenes George R. Pettit, Mathew D. Minardi, Heidi J. Rosenberg, Ernest Hamel, Michael C. Bibby, Sandie W. Martin, M. Katherine Jung, Robin K. Pettit, Timothy J. Cuthbertson, and Jean-Charles Chapuis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-bromoboldine C19H20BrNO4 ÏàËÆ¶È:63.1% Journal of Natural Products 2000 63 480-484 Halogenated Boldine Derivatives with Enhanced Monoamine Receptor Selectivity Eduardo M. Sobarzo-S¨¢nchez, Jeannette Arbaoui, Philippe Protais, and Bruce K. Cassels Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . Hemiargine B C19H19NO4 ÏàËÆ¶È:63.1% Journal of Chinese Pharmaceutical Sciences 2003 12 711-221 The Alkaloids from Leaves of Croton hemiargyerius var. gymnodiscus Lin Wen-han , Fu Hong-zheng, Li Jun, Cheng Gang, and Roeder Abarnes Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . (+)-isolariciresinol ÏàËÆ¶È:63.1% China Journal of Chinese Materia Medica 2009 34 2197-2199 Chemical constituents from fruits of Ailanthus altissima ZHAO Chunchao, SHAO Jianhua, LIXian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . N-transferuloyl-3-methyldopamine C19H21NO5 ÏàËÆ¶È:63.1% Acta Pharmaceutica Sinica 2004 Vol 39 598-600 Studies on the alkaloids from Salsola collina Pall. ZHAO Yun-xue; DING Xing-bao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . (6S,6aS,M)-Corydine hydrochloride ÏàËÆ¶È:63.1% Phytochemistry 2010 71 469-478 Aporphine and bisaporphine alkaloids from Aristolochia lagesiana var. intermedia Marcia L.R. Ferreira, Inara C. de Pascoli, Isabele R. Nascimento, Julio Zukerman-Schpector, Lucia M.X. Lopes Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 4-[2-(6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-ethyl]phenylamine C19H24N2O2 ÏàËÆ¶È:63.1% Bioorganic & Medicinal Chemistry 2009 17 2524-2535 Synthesis and biological evaluation of a small molecule library of 3rd generation multidrug resistance modulators Werner Klinkhammer, Henrik M¨¹ller, Christoph Globisch, Ilza K. Pajeva, Michael Wiese Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 3-bromoboldine C19H20BrNO4 ÏàËÆ¶È:63.1% Medicinal Chemistry Research 2012 21 3133-3139 Synthesis and reactive oxygen species scavenging activity of halogenated alkaloids from boldine Lara Mili¨¢n • Rafael Ballesteros • Mar¨ªa Jes¨²s Sanz •Mar¨ªa Amparo Bl¨¢zquez Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . laurotetanine ÏàËÆ¶È:63.1% Biochemical Systematics and Ecology 2013 51 331-334 Isoquinoline alkaloids from the leaves of Xylopia laevigata (Annonaceae) Emmanoel Vilaça Costa, L¨ªvia Macedo Dutra, Angelita Nepel, Andersson Barison Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 4-(3,11-dimethoxy-5,6,8,9-tetrahydro-dibenzo[c,h]acridin-7-yl)-2-methoxy-phenol C30H27NO4 ÏàËÆ¶È:63.1% Journal of Heterocyclic Chemistry 2013 50 1230-1235 Sulfamic Acid-Catalyzed Multicomponent One-Pot Synthesis of Poly-Substituted Pyridines and Their Antimicrobial Activity B. Janardhan, S. Vijayalaxmi and B. Rajitha Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 15 ÏàËÆ¶È:60.8% Phytochemistry 1997 45 1235-1247 Bibenzyl derivatives from Pellia epiphylla Frank Cullmann, Hans Becker, Enrique Pandolfi, Eckard Roeckner, Theophil Eicher Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . (+)-laudanidine C20H25NO4 ÏàËÆ¶È:60% Phytochemistry 2003 711-720 Characterisation of alkaloids from some Australian Stephania (Menispermaceae) species Joanne T. Blanchfield, Donald P.A. Sands, Colin H.L. Kennard, Karl A. Byriel,William Kitching Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . acutissimalignan B C20H20O6 ÏàËÆ¶È:60% Journal of Natural Products 2008 71(4) 655-663 Dichapetalin-Type Triterpenoids and Lignans from the Aerial Parts of Phyllanthus acutissima Patoomratana Tuchinda, Jittra Kornsakulkarn, Manat Pohmakotr, Palangpon Kongsaeree, Samran Prabpai, Chalobon Yoosook, Jitra Kasisit, Chanita Napaswad, Samaisukh Sophasan, and Vichai Reutrakul Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 9,9¡ä-O-di-(Z)-feruloyl-(-)-secoisolariciresinol C40H42O12 ÏàËÆ¶È:60% Journal of Natural Products 2008 71(6) 1016-1021 Dihydroagarofuranoid Sesquiterpenes, a Lignan Derivative, a Benzenoid,and Antitubercular Constituents from the Stem of Microtropis japonica Jih-Jung Chen, Chang-Syun Yang, Chien-Fang Peng, Ih-Sheng Chen, and Chang-Ling Miaw Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . (7¡äS,8¡äS)-nocomtal C20H20O7 ÏàËÆ¶È:60% Journal of Natural Products 2008 71(2) 212-217 Neolignans, a Coumarinolignan, Lignan Derivatives, and a Chromene:Anti-inflammatory Constituents from Zanthoxylum avicennae Jih-Jung Chen, Tzu-Ying Wang, and Tsong-Long Hwang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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